Mouse neural crest cells secrete both urokinase-type and tissue-type plasminogen activators in vitro
Neural tubes of E8-5 day mouse embryos were dissected and cultured in serum substitute-supplemented medium to allow the emigration of neural crest cells. After 48 h of culture the neural tubes were removed. The neural crest cells were then cultured for 12 h in serum-free medium, and their culture su...
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Veröffentlicht in: | Development (Cambridge) 1989-08, Vol.106 (4), p.685-690 |
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description | Neural tubes of E8-5 day mouse embryos were dissected and cultured in serum substitute-supplemented medium to allow the emigration of neural crest cells. After 48 h of culture the neural tubes were removed. The neural crest cells were then cultured for 12 h in serum-free medium, and their culture supernatant was studied by electrophoresis and zymography. The cultured cells were shown to secrete both urokinase-type and tissue-type plasminogen activators. When the truncal neural tube was divided in four equal segments, the secretion pattern of the two types of plasminogen activators was similar for the cells from the three most anterior segments; cells having migrated from the most caudal one, i.e. consisting of the neural plate, secreted a higher level of urokinase-type plasminogen activator. The secretion in vitro of plasminogen activators by neural crest cells is in accord with the postulated importance of these proteases in cellular migration. |
doi_str_mv | 10.1242/dev.106.4.685 |
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After 48 h of culture the neural tubes were removed. The neural crest cells were then cultured for 12 h in serum-free medium, and their culture supernatant was studied by electrophoresis and zymography. The cultured cells were shown to secrete both urokinase-type and tissue-type plasminogen activators. When the truncal neural tube was divided in four equal segments, the secretion pattern of the two types of plasminogen activators was similar for the cells from the three most anterior segments; cells having migrated from the most caudal one, i.e. consisting of the neural plate, secreted a higher level of urokinase-type plasminogen activator. The secretion in vitro of plasminogen activators by neural crest cells is in accord with the postulated importance of these proteases in cellular migration.</description><identifier>ISSN: 0950-1991</identifier><identifier>EISSN: 1477-9129</identifier><identifier>DOI: 10.1242/dev.106.4.685</identifier><identifier>PMID: 2562663</identifier><language>eng</language><publisher>England: The Company of Biologists Limited</publisher><subject>Animals ; Cells, Cultured ; Culture Media, Serum-Free ; Electrophoresis, Polyacrylamide Gel ; Mice ; Neural Crest - embryology ; Tissue Plasminogen Activator - biosynthesis ; Tissue Plasminogen Activator - metabolism ; Urokinase-Type Plasminogen Activator - biosynthesis ; Urokinase-Type Plasminogen Activator - metabolism</subject><ispartof>Development (Cambridge), 1989-08, Vol.106 (4), p.685-690</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c271t-1b662f2c27832c2dc674f28efd6ae94e48e9452abc39223c87bd2f7c1969ca6a3</citedby><cites>FETCH-LOGICAL-c271t-1b662f2c27832c2dc674f28efd6ae94e48e9452abc39223c87bd2f7c1969ca6a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3665,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2562663$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Menoud, P A</creatorcontrib><creatorcontrib>Debrot, S</creatorcontrib><creatorcontrib>Schowing, J</creatorcontrib><title>Mouse neural crest cells secrete both urokinase-type and tissue-type plasminogen activators in vitro</title><title>Development (Cambridge)</title><addtitle>Development</addtitle><description>Neural tubes of E8-5 day mouse embryos were dissected and cultured in serum substitute-supplemented medium to allow the emigration of neural crest cells. After 48 h of culture the neural tubes were removed. The neural crest cells were then cultured for 12 h in serum-free medium, and their culture supernatant was studied by electrophoresis and zymography. The cultured cells were shown to secrete both urokinase-type and tissue-type plasminogen activators. When the truncal neural tube was divided in four equal segments, the secretion pattern of the two types of plasminogen activators was similar for the cells from the three most anterior segments; cells having migrated from the most caudal one, i.e. consisting of the neural plate, secreted a higher level of urokinase-type plasminogen activator. The secretion in vitro of plasminogen activators by neural crest cells is in accord with the postulated importance of these proteases in cellular migration.</description><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Culture Media, Serum-Free</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Mice</subject><subject>Neural Crest - embryology</subject><subject>Tissue Plasminogen Activator - biosynthesis</subject><subject>Tissue Plasminogen Activator - metabolism</subject><subject>Urokinase-Type Plasminogen Activator - biosynthesis</subject><subject>Urokinase-Type Plasminogen Activator - metabolism</subject><issn>0950-1991</issn><issn>1477-9129</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkEFP3DAQha0KRJdtjxwr-cSJLLaTOPERIWgrbcUFzpbjTHZNkzj1OIv49_VqI8RlZp7m6ZPeI-SKsw0Xhbht4bDhTG6KjazLL2TFi6rKFBfqjKyYKlnGleJfySXiK2Msl1V1QS5EKYWU-Yq0f_yMQEeYg-mpDYCRWuh7pAhJRaCNj3s6B__XjQYhi-8TUDO2NDrEedFTb3Bwo9_BSI2N7mCiD0jdSA8uBv-NnHemR_i-7DV5eXx4vv-VbZ9-_r6_22ZWVDxmvJFSdCKJOk-ztbIqOlFD10oDqoCiTrMUprG5EiK3ddW0oqssV1JZI02-Jtcn7hT8vzlF0YPDYxozQoqpeVmw8khfk-xktMEjBuj0FNxgwrvmTB9b1anVdEtd6NRq8v9YwHMzQPvhXmpM_5vTf-92-zcXQDfO937nMOIRBb2fPuH-A9achRE</recordid><startdate>198908</startdate><enddate>198908</enddate><creator>Menoud, P A</creator><creator>Debrot, S</creator><creator>Schowing, J</creator><general>The Company of Biologists Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope></search><sort><creationdate>198908</creationdate><title>Mouse neural crest cells secrete both urokinase-type and tissue-type plasminogen activators in vitro</title><author>Menoud, P A ; Debrot, S ; Schowing, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c271t-1b662f2c27832c2dc674f28efd6ae94e48e9452abc39223c87bd2f7c1969ca6a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Animals</topic><topic>Cells, Cultured</topic><topic>Culture Media, Serum-Free</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Mice</topic><topic>Neural Crest - embryology</topic><topic>Tissue Plasminogen Activator - biosynthesis</topic><topic>Tissue Plasminogen Activator - metabolism</topic><topic>Urokinase-Type Plasminogen Activator - biosynthesis</topic><topic>Urokinase-Type Plasminogen Activator - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Menoud, P A</creatorcontrib><creatorcontrib>Debrot, S</creatorcontrib><creatorcontrib>Schowing, J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>Development (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Menoud, P A</au><au>Debrot, S</au><au>Schowing, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mouse neural crest cells secrete both urokinase-type and tissue-type plasminogen activators in vitro</atitle><jtitle>Development (Cambridge)</jtitle><addtitle>Development</addtitle><date>1989-08</date><risdate>1989</risdate><volume>106</volume><issue>4</issue><spage>685</spage><epage>690</epage><pages>685-690</pages><issn>0950-1991</issn><eissn>1477-9129</eissn><abstract>Neural tubes of E8-5 day mouse embryos were dissected and cultured in serum substitute-supplemented medium to allow the emigration of neural crest cells. After 48 h of culture the neural tubes were removed. The neural crest cells were then cultured for 12 h in serum-free medium, and their culture supernatant was studied by electrophoresis and zymography. The cultured cells were shown to secrete both urokinase-type and tissue-type plasminogen activators. When the truncal neural tube was divided in four equal segments, the secretion pattern of the two types of plasminogen activators was similar for the cells from the three most anterior segments; cells having migrated from the most caudal one, i.e. consisting of the neural plate, secreted a higher level of urokinase-type plasminogen activator. The secretion in vitro of plasminogen activators by neural crest cells is in accord with the postulated importance of these proteases in cellular migration.</abstract><cop>England</cop><pub>The Company of Biologists Limited</pub><pmid>2562663</pmid><doi>10.1242/dev.106.4.685</doi><tpages>6</tpages></addata></record> |
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issn | 0950-1991 1477-9129 |
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subjects | Animals Cells, Cultured Culture Media, Serum-Free Electrophoresis, Polyacrylamide Gel Mice Neural Crest - embryology Tissue Plasminogen Activator - biosynthesis Tissue Plasminogen Activator - metabolism Urokinase-Type Plasminogen Activator - biosynthesis Urokinase-Type Plasminogen Activator - metabolism |
title | Mouse neural crest cells secrete both urokinase-type and tissue-type plasminogen activators in vitro |
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